A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4433938



Internal ID21395940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167126818..167131469hg38UCSC Ensembl
chr3:166844606..166849257hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg384652
hg194652
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv536n172
Supporting Variantsnssv15751753
SamplesNB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4433938
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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